> For the complete documentation index, see [llms.txt](https://help.connected.illumina.com/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://help.connected.illumina.com/emedgene/release-notes/change_log/change_log_workbench_228.md).

# Change log workbench 2.28

## **Features:**

* Support for interpreting STRs - annotation with 1K genomes and gnomAD, custom visualization, related cases
* Support for interpreting SV deletions and duplications. ACMG automated classification tool applies to SV del/dups.
* Emedgene Curate supports gene curation - save and view gene interpretations, save preferred transcripts.
* Emedgene Curate - new private networking component for opted in laboratories
* ACMG classification improvements
* In analysis tools disease column, hover to view see all related diseases
* New Filter under Variant Effect, Advanced, Curate - select pathogenicity
* View allele frequency full decimal number
* Var Page | Quality Tab | Add tooltip for quality parameter threshold
* Var Page | Option to import variant interpretation summary from Curate
* Header update - added Illumina logo

## **Bug fixes:**

* Export variant to Curate bug fix
* Organization Settings | Management | Fix broken create group and add users link
* Analysis Tools | Filters | Compound heterozygous filter now supports CNV del/SNV
* Analysis Tools | Filters | ACMG | VUS renamed Uncertain
* Reporting | View reports for past cases even if template has been archived
* API | Fixed error where case type wasn’t saved


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